chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1252808371252808372GC28GENIChomozygous108612662
1252809968252809968AAT18GENIChomozygous132542002
1252810111252810111A24GENIChomozygous132542003
1252810225252810226TC29GENIChomozygous108612664
1252810315252810316TC21GENIChomozygous109020099
1252810054252810055TC15GENIChomozygous109020096
1252808766252808767GT28GENIChomozygous109020094
1252810211252810212AC30GENIChomozygous109020097
1252810307252810308GA23GENIChomozygous109020098
1252810093252810094A21GENIChomozygous127504327
1252810360252810361GA20GENIChomozygous109020100
1252810444252810445AG23GENIChomozygous109020101
1252810590252810591AG32GENIChomozygous109020102
1252810796252810797CT19GENIChomozygous109020103
1252811030252811031CG14GENIChomozygous109020107
1252810934252810935TC18GENIChomozygous109020104
1252810971252810972AG20GENIChomozygous109020105
1252811000252811001GA17GENIChomozygous109020106
1252810874252810875CT16GENIChomozygous120516011
1252810875252810876TC16GENIChomozygous120516012
1252811092252811093GA11GENIChomozygous109020108
1252811142252811143GA9GENIChomozygous109020109
1252811182252811183G11GENIChomozygous132542004
1252811286252811286AAAG19GENIChomozygous132542005